Cluster Randomised Trials (CTM209)
Aims
To understand the key features in the design, analysis and reporting of cluster randomised trials. Trials in which individuals are randomised in groups (clusters) are being increasingly utilised, especially in the fields of infectious diseases, implementation research, and public health and complex interventions. This module will consider the advantages and disadvantages of the use of cluster trials, with particular emphasis on statistical considerations for their design and analysis, as well as the implications for informed consent and reporting.
Credits
15 credits are offered on successful completion of this module.
Prerequisites and Selection
Those wishing to study this module should have regular access to the internet to benefit from library facilities, participate in web-based conference discussions and submit assignments.
Prior knowledge and experience of clinical trials is needed - please see the Module Outline for more details.
Students must meet the required standard of English required to study this course. Details can be found here.
2012-13 Fee
The tuition fee for this module is £1,655.
Module Outline
A full outline of the module can be downloaded here as a PDF.
